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Bard® Adult/Pediatric Feeding Tube 0036420Recalls & reported problems

C. R. Bard, Inc. · Bard® Adult/Pediatric Feeding Tube · Class 2

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00801741034428), received between Feb 28, 2019 and Feb 28, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Deformation Due to Compressive Stress” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Deformation Due to Compressive Stress1
  • Difficult to Remove1
  • Material Deformation1

Patient problems

  • No Consequences Or Impact To Patient1
  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionFeb 28, 2019Difficult to Remove; Deformation Due to Compressive Stress; Material Deformation; Deformation Due to Compressive Stress

    IT WAS REPORTED THAT THE TUBE BECAME KINKED WHILE IN USE AND CAUSED IT TO BE DIFFICULT TO REMOVE.

    Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient

    MAUDE report 8377344 ↗

Other TUBE, FEEDING devices

All TUBE, FEEDING devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.